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4-Cyanophenol → 4-(2-Morpholin-4-ylethoxy)benzonitrile

HRID 977140
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HRID 977140 반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1)#[N:2].[H-].[Na+].Cl[CH2:13][CH2:14][N:15]1[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1>CN(C=O)C>[N:15]1([CH2:14][CH2:13][O:9][C:6]2[CH:7]=[CH:8][C:3]([C:1]#[N:2])=[CH:4][CH:5]=2)[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 130194-CyanophenolHCID 24758Sodium hydrideHCID 767274-(2-Chloroethyl)morpholine

생성물 1

HCID 29940744-(2-Morpholin-4-ylethoxy)benzonitrile수율 97%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

To a solution of 4-cyanophenol (5.95 g, 0.05 mol) in DMF (35 mL) at 0° C. was added 60% NaH (2.2 g, 0.055 mol). The reaction mixture was stirred at 0° C. for 15 minutes, then at room temperature for 15 minutes and then N-(2-chloroethyl)morpholine (prepared from 11.16 g, 0.06 mol of the hydrochloride salt) was added and the reaction mixture was stirred at room temperature for about 2 days. There was still a small amount of starting material present so the reaction mixture was heated on a steam bath for 4 hours. The reaction mixture was cooled to room temperature and then the solvent was removed. Ice-water was added to the residue and the solid which precipitated was collected by filtration and dried to afford 11.3 g (97%) of 4-[2-(4-morpholinyl)ethoxy]benzonitrile.

후처리

  1. waitat room temperature for 15 minutes
  2. additionwas added
  3. stirringthe reaction mixture was stirred at room temperature for about 2 days
  4. temperaturewas heated on a steam bath for 4 hours
  5. temperatureThe reaction mixture was cooled to room temperature
  6. customthe solvent was removed
  7. additionIce-water was added to the residue
  8. customthe solid which precipitated
  9. filtrationwas collected by filtration
  10. customdried

출처 및 근거

ORD 기록
ord-41405cb76bf6444184e7c4c155b3495d
출처 데이터셋
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05614530

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